Statins and atherosclerotic cardiovascular outcomes in patients on incident dialysis and with atherosclerotic heart disease.
Adult
Age Factors
Aged
Aged, 80 and over
Atherosclerosis
/ drug therapy
Cause of Death
Coronary Disease
/ drug therapy
Female
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors
/ therapeutic use
Kaplan-Meier Estimate
Kidney Failure, Chronic
/ therapy
Kidney Transplantation
Male
Middle Aged
Myocardial Infarction
/ epidemiology
Propensity Score
Renal Dialysis
Stroke
/ epidemiology
Journal
American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465
Informations de publication
Date de publication:
01 2021
01 2021
Historique:
received:
14
10
2020
accepted:
14
10
2020
pubmed:
24
10
2020
medline:
29
1
2021
entrez:
23
10
2020
Statut:
ppublish
Résumé
Statins failed to reduce cardiovascular (CV) events in trials of patients on dialysis. However, trial populations used criteria that often excluded those with atherosclerotic heart disease (ASHD), in whom statins have the greatest benefit, and included outcome composites with high rates of nonatherosclerotic CV events that may not be modified by statins. Here, we study whether statin use associates with lower atherosclerotic CV risk among patients with known ASHD on dialysis, including in those likely to receive a kidney transplant, a group excluded within trials but with lower competing mortality risks. Using data from the United States Renal Data System including Medicare claims, we identified adults initiating dialysis with ASHD. We matched statin users 1:1 to statin nonusers with propensity scores incorporating hard matches for age and kidney transplant listing status. Using Cox models, we evaluated associations of statin use with the primary composite of fatal/nonfatal myocardial infarction and stroke (including within prespecified subgroups of younger age [<50 years] and waitlisting status); secondary outcomes included all-cause mortality and the composite of all-cause mortality, nonfatal myocardial infarction, or stroke. Of 197,716 patients with ASHD, 47,562 (24%) were consistent statin users from which we created 46,186 matched pairs. Over a median 662 days, statin users had similar risk of fatal/nonfatal myocardial infarction or stroke overall (hazard ratio [HR] 1.00, 95% CI 0.97-1.02), or in subgroups (age< 50 years [HR = 1.05, 95% CI 0.95-1.17]; waitlisted for kidney transplant [HR 0.99, 95% CI 0.97-1.02]). Statin use was modestly associated with lower all-cause mortality (HR 0.96, 95% CI 0.94-0.98; E value = 1.21) and, similarly, a modest lower composite risk of all-cause mortality, nonfatal myocardial infarction, or stroke over the first 2 years (HR 0.90, 95% CI 0.88-0.91) but attenuated thereafter (HR 0.98, 95% CI 0.96-1.01). Our large observational analyses are consistent with trials in more selected populations and suggest that statins may not meaningfully reduce atherosclerotic CV events even among incident dialysis patients with established ASHD and those likely to receive kidney transplants.
Identifiants
pubmed: 33096103
pii: S0002-8703(20)30341-0
doi: 10.1016/j.ahj.2020.10.055
pmc: PMC9011977
mid: NIHMS1794332
pii:
doi:
Substances chimiques
Hydroxymethylglutaryl-CoA Reductase Inhibitors
0
Types de publication
Journal Article
Observational Study
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
36-44Subventions
Organisme : NIDDK NIH HHS
ID : R01 DK111952
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002553
Pays : United States
Commentaires et corrections
Type : ErratumIn
Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Références
N Engl J Med. 2009 Apr 2;360(14):1395-407
pubmed: 19332456
Atherosclerosis. 2017 Dec;267:158-166
pubmed: 28985950
Kidney Int. 2014 Jun;85(6):1303-9
pubmed: 24552851
Lancet. 2019 Feb 2;393(10170):407-415
pubmed: 30712900
Circulation. 1993 Jun;87(6):1781-91
pubmed: 8504494
Ann Intern Med. 2014 Feb 4;160(3):182
pubmed: 24323134
Int J Cardiol. 2013 Oct 9;168(4):4155-9
pubmed: 23928338
Lancet. 2011 Jun 25;377(9784):2181-92
pubmed: 21663949
Medicine (Baltimore). 2017 Feb;96(5):e5924
pubmed: 28151871
Am J Transplant. 2004 Jun;4(6):988-95
pubmed: 15147434
JAMA Intern Med. 2019 Oct 01;179(10):1316-1324
pubmed: 31282924
Am Heart J. 2010 Nov;160(5):785-794.e10
pubmed: 21095263
Lancet. 2003 Jun 14;361(9374):2024-31
pubmed: 12814712
Lancet. 2010 Nov 13;376(9753):1670-81
pubmed: 21067804
JAMA Netw Open. 2018 Oct 5;1(6):e182311
pubmed: 30646217
N Engl J Med. 2005 Jul 21;353(3):238-48
pubmed: 16034009
Kidney Int. 2010 Jan;77(2):141-51
pubmed: 19907414
J Am Coll Cardiol. 2019 Oct 8;74(14):1823-1838
pubmed: 31582143
N Engl J Med. 2005 Apr 7;352(14):1425-35
pubmed: 15755765
J Am Coll Cardiol. 2011 Nov 29;58(23):2432-46
pubmed: 22055990
Am J Kidney Dis. 2005 Jan;45(1):119-26
pubmed: 15696451
Lancet. 1994 Nov 19;344(8934):1383-9
pubmed: 7968073
J Natl Cancer Inst. 2017 Aug 1;109(8):
pubmed: 28376195
Hypertension. 2001 Oct;38(4):938-42
pubmed: 11641313
Lancet. 2002 Jul 6;360(9326):7-22
pubmed: 12114036
Prog Cardiovasc Dis. 1993 May-Jun;35(6):435-54
pubmed: 8497659
Ann Intern Med. 2017 Aug 15;167(4):268-274
pubmed: 28693043